2003
DOI: 10.1016/s0003-2670(03)00922-x
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Determination of naproxen in pharmaceuticals by differential pulse voltammetry at a platinum electrode

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Cited by 79 publications
(51 citation statements)
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“…The analytical frequency estimated in this amperometric recording is higher than 90 h -1 (much superior than the DPV methods previously reported). 12,13 A linear behavior, with a good correlation coefficient (R > 0.99), was observed from 10 to 100 µmol L -1 naproxen with similar slope values for both curves (0.357 and 0.336 µA L µmol -1 ). Electrode fouling was not verified between injections of standard solutions, as evidenced by the fact that current responses were not diminished during amperometric measurements due to the application of a cleaning potential pulse (+1.0 V) using the pulsed amperometric detection technique.…”
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confidence: 68%
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“…The analytical frequency estimated in this amperometric recording is higher than 90 h -1 (much superior than the DPV methods previously reported). 12,13 A linear behavior, with a good correlation coefficient (R > 0.99), was observed from 10 to 100 µmol L -1 naproxen with similar slope values for both curves (0.357 and 0.336 µA L µmol -1 ). Electrode fouling was not verified between injections of standard solutions, as evidenced by the fact that current responses were not diminished during amperometric measurements due to the application of a cleaning potential pulse (+1.0 V) using the pulsed amperometric detection technique.…”
mentioning
confidence: 68%
“…However, both electroanalytical procedures employed non-aqueous electrolyte. 12,13 Figure 4 presents amperometric responses for triplicate injections of solutions containing increasing concentrations of naproxen (a-e: 10-100 µmol L -1 ). The respective calibration curves (increasing and decreasing order) are also presented (inset).…”
Section: Resultsmentioning
confidence: 99%
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“…Several analytical methods have been reported for the determination of naproxen in pharmaceutical preparations including UV-visible spectrophotomery, [3][4][5] spectrofluorimetry, [6][7][8] room temperature phosphorimetry, 9,10 voltametry, 11 high-performance liquid chromatography, [12][13][14] capillary electrophoresis, 15,16 coulometry 17 and oscilometric titration. 18 However, most of these techniques are timeconsuming, involving the use of organic solvents or require expensive and sophisticated instruments and for this reason they are not suitable for routine analysis.…”
Section: Introductionmentioning
confidence: 99%